PARIS: Lab
scientists on Wednesday reported that for the first time they had taken skin
cells from patients who had suffered heart failure and turned them into cells
that could repair damaged cardiac muscle.
The technique has so far been tested on rats and it
could take up to a decade of problem-solving before trials can go ahead on
humans, the scientists cautioned.
Even so, it marks an important advance in the quest
for replacement cells to treat tissue affected by disease, said the scientists
who developed the technique in Israel.
The research uses a method called human-induced
pluripotent stem cells, or hiPSCs, a recently-discovered source that is viewed
as an exciting and less controversial research alternative to embryonic stem
cells.
It entails taking cells from a patient and
introducing genes to the cell nucleus. Helped by a chemical
"cocktail," these genes then act as switches which reprogramme the
cells back to their versatile, youthful state.
The ultimate goal is that if a patient's own cells
are used as the replenishment source, they will be recognised as friendly by
the immune system and not be attacked.
Recent studies have shown it is possible to derive
hiPSCs from young and healthy people and that these are capable of transforming
into heart cells.
But until now, hiPSCs could not be obtained from
elderly and diseased patients.
Nor have researchers been able to show that heart
cells created from hiPSCs can integrate with existing heart tissue.
"What is new and exciting about our research is
that we have shown that it's possible to take skin cells from an elderly
patient with advanced heart failure and end up with his own beating cells in a
laboratory dish that are healthy and young," said Lior Gepstein, a
professor of cardiology at the Technion-Israel Institute of Technology and
Rambam Medical Center in Haifa, Israel.
It is "the equivalent to the stage of his
heart cells when he was just born," Gepstein said in a statement.
Gepstein's team took skin cells from two men aged
51 and 61 who had suffered heart failure and reprogrammed them by delivering
three genes called Sox2, Klf4 and Oct4, followed by a molecule called valproic
acid.
The method did not include a gene called c-Myc,
which has roused concern because it has been found to cause tumours.
The resulting hiPSCs were cultured together with
pre-existing cardiac tissue and then grafted into healthy rat hearts, where
they appeared to integrate successfully.
Still unclear, though, is whether heart cells
derived from the same patient will be accepted by the immune system.
"One of the obstacles in dealing with this
issue is that, at this stage, we can only transplant human cells into animal
models and so we have to treat the animals with immunosuppressive drugs so the
cells won't be rejected," said Gepstein.
The study is published online in the European Heart
Journal, published by the European Society of Cardiology.
- AFP/wm
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